FEIBA Reconstitution Volume Reduction and Faster Infusion Study (FEIBA STAR)

NCT02764489 | Completed Phase 3 Results FDA Drug

• 2 other identifiers: 0915012015-005781-39
• Study Type: interventional
• Target: 45
• Locations: 3 countries
• Sites: 3

Brief Summary

The purpose of this study is to:

• 1\. To evaluate the tolerability and safety of infusing reduced volume Factor Eight Inhibitor Bypassing Activity (FEIBA) at the standard infusion rate of 2 U/kg/min
• 2\. To evaluate the tolerability and safety of infusing reduced volume FEIBA at increased rates of 4 and 10 U/kg/min, in comparison to the standard rate of 2 U/kg/min at the regular volume

Conditions

Hemophilia A or B With Inhibitors

Outcome Measures

Primary Outcomes (7)

• Number of Participants With Any Treatment Emergent Adverse Event (TEAE)

  An adverse event (AE) is any untoward medical occurrence in a clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment.

  From first dose of study drug up to 7 days after the end of infusion (up to Day 41)

• Number of Participants With Any Hypersensitivity Reaction

  Number of participants with AEs particular to allergic-type hypersensitivity reactions were assessed. Clinical manifestations of hypersensitivity reactions included, but was not limited to skin rash, pruritus (itching), urticaria (hives), angioedema (for example, swelling of the lips and/or tongue) and anaphylactic reaction.

  From first dose of study drug up to 7 days after the end of infusion (up to Day 41)

• Number of Participants With Any Thromboembolic Event

  Participants with adverse events related to thromboembolic event were reported. Clinical manifestations of thromboembolic events included, but was not limited to myocardial infarction, deep vein thrombosis, pulmonary embolism, stroke and transitory ischemic attack.

  From first dose of study drug up to 7 days after the end of infusion (up to Day 41)

• Number of Participants With Any Infusion Site Reaction

  Infusion sites were monitored for pain, tenderness, erythema, and swelling. Infusion site evaluations were made by clinical staff or by the participant or caregiver.

  From first dose of study drug up to 7 days after the end of infusion (up to Day 41)

• Number of Participants With AEs Leading to Study Discontinuation

  From first dose of study drug up to 7 days after the end of infusion (up to Day 41)

• Number of Participants With Vital Signs Considered as AEs

  Number of participants with vital signs considered as AEs were assessed. Vital signs included body temperature (degree Celsius or degrees Fahrenheit \[°C or °F\]), respiratory rate (breaths/min), pulse rate (beats/min), and systolic and diastolic blood pressure (millimeter of mercury \[mmHg\]).

  From first dose of study drug up to 7 days after the end of infusion (up to Day 41)

• Number of Participants With Laboratory Assessments Considered as AEs

  Number of participants with Laboratory Assessments considered as AEs were assessed. Laboratory assessments included hematology, clinical chemistry, coagulation testing, serological testing, pregnancy testing, cluster differentiation 4 (CD4).

  From first dose of study drug up to 7 days after the end of infusion (up to Day 41)

Study Arms (2)

Part 1:FEIBA 85±15 U/kg at Regular Volume Then 50% Reduced Volume at 2 U/kg/min Rate or Vice Versa

EXPERIMENTAL

Participants who were eligible were randomized to receive: 3 infusions (infusions 1, 2 and 3) of factor eight inhibitor bypassing activity (FEIBA) 85 ± 15 U/kg, reconstituted in regular volume sterile water for injection (SWFI) followed by 3 infusions (infusions 4, 5 and 6) of FEIBA 85 ± 15 U/kg reconstituted in 50% reduced volume SWFI (Sequence A) or: 3 infusions (infusions 1, 2 and 3) of FEIBA 85 ± 15 U/kg, reconstituted in 50% reduced volume SWFI, followed by 3 infusions of FEIBA 85 ± 15 U/kg, reconstituted in regular volume SWFI (Sequence B). All infusions in Part 1 were given at the standard infusion rate of 2 U/kg/min.

Biological: FEIBA

Part 2:FEIBA 85±15U/kg 50% Reduced Volume at 4U/kg/min Rate Then at 10U/kg/min Rate

EXPERIMENTAL

Participants who completed Part 1, received FEIBA 85 ± 15 U/kg, reconstituted in 50% reduced volume SWFI at an increased rate of 4 U/kg/min for infusions 7, 8, and 9, followed by FEIBA 85 ± 15 U/kg, reconstituted in 50% reduced volume SWFI at an increased rate of 10 U/kg/min for infusions 10, 11, and 12.

Biological: FEIBA

Interventions

FEIBA BIOLOGICAL

Anti-inhibitor Coagulant Complex Nanofiltered (activated prothrombin complex concentrate \[APCC\]), FEIBA NF.

Also known as: FEIBA NF., AICC, anti-inhibitor coagulant complex, Anti-inhibitor Coagulant Complex Nanofiltered (activated prothrombin complex concentrate [APCC]), APCC, Activated prothrombin complex concentrate

Part 1:FEIBA 85±15 U/kg at Regular Volume Then 50% Reduced Volume at 2 U/kg/min Rate or Vice Versa; Part 2:FEIBA 85±15U/kg 50% Reduced Volume at 4U/kg/min Rate Then at 10U/kg/min Rate

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Greater than or equal to (\> or =) 18 to less than or equal to (\< or =) 65 years old at the time of screening.
• Hemophilia A or B of any severity, with a documented \> or = 3 months history of inhibitors (\> or = 0.6 Bethesda units \[BU\]) requiring the use of bypassing agents (FEIBA or rFVIIa) prior to screening. Inhibitor level will be tested at screening if no documented history is available.
• Hepatitis C virus (HCV) negative, either by antibody testing or polymerase chain reaction (PCR); or HCV positive with stable liver disease.
• Human immune deficiency virus (HIV) negative; or HIV positive with stable disease and CD4 count \> or = 200 cells per cubic millimetre (cell/mm3) at screening.
• Adequate venous access.
• Willing and able to comply with the requirements of the protocol.
• If a female of childbearing potential, must have a negative blood pregnancy test and agrees to employ adequate birth control measures for the duration of the study, such as: a. Abstain from sexual intercourse, b. Use a reliable method of contraception (contraception such as an intrauterine device, barrier method \[e.g., diaphragm or sponge; female condom not permitted\] with spermicide, oral contraceptive, injectable progesterone, sub dermal implant), and have their male partner use a condom
• If female of non-childbearing potential, confirmed at screening by fulfilling 1 of the following criteria:
• Postmenopausal, defined as amenorrhea for at least 12 months following cessation of all exogenous hormonal treatments and with follicle-stimulating hormone levels within the laboratory-defined postmenopausal range or postmenopausal with amenorrhea for at least 24 months and on hormonal replacement therapy.
• Documentation of irreversible surgical sterilization by hysterectomy, bilateral oophorectomy, bilateral tubal ligation (with no subsequent pregnancy at least 1 year from bilateral tubal ligation), or bilateral salpingectomy.

You may not qualify if:

• Known hypersensitivity to FEIBA or any of its components.
• Advanced liver disease (e.g., liver biopsy confirmed diagnosis of cirrhosis, portal vein hypertension, ascites, prothrombin time \[PT\] 5 seconds above upper limit of normal).
• Planned elective surgery during participation in this study (excluding minor procedures that will not need preventative bleeding treatments, such as exchanges of peripherally inserted central catheters).
• Platelet count less than (\<) 100,000/ microliter (μL).
• Taking Emicizumab (Hemlibra) for bleed prevention.
• Clinical or laboratory evidence of disseminated intravascular coagulation based on medical history.
• Prior history or evidence of thromboembolic event: acute myocardial infarction, deep vein thrombosis, pulmonary embolism, etc.
• Diagnosis of advanced atherosclerosis, malignancy, and/or other diseases that may increase the participant's risk of thromboembolic complications.
• Participant is taking any immunomodulating drug (e.g., corticosteroid agents at a dose equivalent to hydrocortisone greater than (\>) 10 milligram per day (mg/day), or α-interferon) within 30 days prior to enrollment except anti-retroviral chemotherapy.
• Herbal supplements that contain anti-platelet activity.
• Participant has participated in another clinical study involving an investigational product (IP) or investigational device within 30 days prior to enrollment or is scheduled to participate in another clinical study involving an IP or investigational device during the course of this study.
• Participant is a family member or employee of the investigator.
• Clinically significant medical, psychiatric or cognitive illness, or recreational drug/alcohol use that, in the opinion of the investigator, would affect participant safety or compliance.

Sponsors & Collaborators

• Baxalta now part of Shire: lead
• Baxalta Innovations GmbH, now part of Shire: collaborator

Study Sites (3)

University Hospital Center Zagreb

Zagreb, 10 000, Croatia

Location

PHI Institute for Transfusion Medicine of Macedonia

Skopje, 1000, North Macedonia

Location

MV Sklifosovskyi Poltava Hematology

Poltava, 36011, Ukraine

Location

Related Links

• To obtain more information on the study, click here/on this link

MeSH Terms

Conditions

Hemophilia A

Interventions

anti-inhibitor coagulant complex

Condition Hierarchy (Ancestors)

Blood Coagulation Disorders, Inherited; Blood Coagulation Disorders; Hematologic Diseases; Hemic and Lymphatic Diseases; Coagulation Protein Disorders; Hemorrhagic Disorders; Genetic Diseases, Inborn; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Results Point of Contact

• Title: Study Director
• Organization: Takeda

TrialDisclosures@takeda.com

+1-877-825-3327

Study Officials

• Study Director

  Shire

  STUDY DIRECTOR

Publication Agreements

• PI is Sponsor Employee: No
• Restriction Type: OTHER
• Restrictive Agreement: Yes

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 11, 2016
• First Posted: May 6, 2016
• Study Start: February 12, 2019
• Primary Completion: December 27, 2021
• Study Completion: December 27, 2021
• Last Updated: February 14, 2023
• Results First Posted: February 9, 2023

Record last verified: 2023-02

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, SAP, ICF, CSR
• Access Criteria: IPD from eligible studies will be shared with qualified researchers according to the criteria and process described on https://vivli.org/ourmember/takeda/. For approved requests, the researchers will be provided access to anonymized data (to respect patient privacy in line with applicable laws and regulations) and with information necessary to address the research objectives under the terms of a data sharing agreement.

Locations

NO (1); CR (1); UA (1)